Testosterone Attenuates Group 2 Innate Lymphoid Cell-Mediated Airway Inflammation.

Cell Rep

Department of Medicine, Vanderbilt University Medical Center, T-1221 Medical Center North, 1161 21(st) Avenue, Nashville, TN 37232, USA; Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Medical Center North, 1161 21(st) Avenue, Nashville, TN 37232, USA. Electronic address:

Published: November 2017

Sex hormones regulate many autoimmune and inflammatory diseases, including asthma. As adults, asthma prevalence is 2-fold greater in women compared to men. The number of group 2 innate lymphoid cells (ILC2) is increased in patients with asthma, and we investigate how testosterone attenuates ILC2 function. In patients with moderate to severe asthma, we determine that women have an increased number of circulating ILC2 compared to men. ILC2 from adult female mice have increased IL-2-mediated ILC2 proliferation versus ILC2 from adult male mice, as well as pre-pubescent females and males. Further, 5α-dihydrotestosterone, a hormone downstream of testosterone, decreases lung ILC2 numbers and IL-5 and IL-13 expression from ILC2. In vivo, testosterone attenuated Alternaria-extract-induced IL-5+ and IL-13+ ILC2 numbers and lung eosinophils by intrinsically decreasing lung ILC2 numbers, as well as by decreasing expression of IL-33 and thymic stromal lymphopoietin (TSLP), ILC2-stimulating cytokines. Collectively, these findings provide a foundational understanding of sexual dimorphism in ILC2 function.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731254PMC
http://dx.doi.org/10.1016/j.celrep.2017.10.110DOI Listing

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Article Synopsis
  • * In a study with Balb/c mice, both male and female mice exhibited increased ILC2s after exposure to IL-33, but females expressed higher levels of important receptors (ST2 and IL-25R) linked to immune responses.
  • * The enhanced type 2 inflammation seen in females is tied to specific ILC2 subsets that have a stronger response capability due to changes driven by the STAT6 pathway, particularly during secondary activation by epithelial-derived cytokines.
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